lithium carbonate

Generic: lithium carbonate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1470
Product ID 50090-1470_f00b7c29-4502-4794-9723-955753196ffd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091544
Listing Expiration 2026-12-31
Marketing Start 2010-12-27

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901470
Hyphenated Format 50090-1470

Supplemental Identifiers

RxCUI
197891
UNII
2BMD2GNA4V

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lithium carbonate (source: ndc)
Generic Name lithium carbonate (source: ndc)
Application Number ANDA091544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1470-0)
source: ndc

Packages (1)

50090-1470-0 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1470-0)

Ingredients (1)

lithium carbonate (300 mg/1)

Linked Drug Pages (1)

Lithium Carbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f00b7c29-4502-4794-9723-955753196ffd", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["3c996da2-c606-4043-9992-5bfb7f9b97a7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1470-0)", "package_ndc": "50090-1470-0", "marketing_start_date": "20141128"}], "brand_name": "Lithium Carbonate", "product_id": "50090-1470_f00b7c29-4502-4794-9723-955753196ffd", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "50090-1470", "generic_name": "Lithium Carbonate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA091544", "marketing_category": "ANDA", "marketing_start_date": "20101227", "listing_expiration_date": "20261231"}